Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference58 articles.
1. Mutations in MYH7 cause multi-minicore disease (MmD) with variable cardiac involvement;Cullup;Neuromuscul Disord,2012
2. Screening and analysis of the mutations on beta-myosin heavy chain gene in 3 Chinese families with hypertrophic cardiomyopathy;Feng;Zhonghua Xin Xue Guan Bing Za Zhi,2011
3. Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy;Homayoun;Neuromuscul Disord,2011
4. MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathy;Muelas;Neurology,2010
5. Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation;Uro-Coste;Neuromuscul Disord,2009
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2. Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre;BMC Pediatrics;2022-01-26
3. The Impact of Next-Generation Sequencing on the Diagnosis, Treatment, and Prevention of Hereditary Neuromuscular Disorders;Molecular Diagnosis & Therapy;2020-09-30
4. Clinical diversity of MYH7 ‐related cardiomyopathies: Insights into genotype–phenotype correlations;American Journal of Medical Genetics Part A;2018-12-27
5. A novel paternally-inherited MYH7 gene variant in brothers with left ventricular non-compaction;IHJ Cardiovascular Case Reports (CVCR);2018-05
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